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Disease: Van Maldergem Wetzburger Verloes syndrome

  • A further patient with van Maldergem syndrome
  • A newborn diagnosed with van Maldergem syndrome
  • Cutis marmorata telangiectatica congenita: a literature review
  • Dchs1-Fat4 regulation of osteogenic differentiation in mouse
  • Hennekam syndrome can be caused by FAT4 mutations and be allelic to Van Maldergem syndrome
  • Intestinal lymphangiectasia-A novel finding in Van Maldergem syndrome challenging the role of lymphedema for the distinction from Hennekam syndrome
  • Mammalian cadherins DCHS1-FAT4 affect functional cerebral architecture
  • Mental retardation with blepharo-naso-facial abnormalities and hand malformations: a new syndrome?
  • Middle ear abnormalities in Van Maldergem syndrome
  • Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical development
  • Van Maldergem syndrome and Hennekam syndrome: Further delineation of allelic phenotypes
  • Van Maldergem syndrome: further characterisation and evidence for neuronal migration abnormalities and autosomal recessive inheritance
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CheckOrphan is a non-profit organization located in Basel, Switzerland and Santa Cruz, California that is dedicated to rare, orphan and neglected diseases. CheckOrphan offers users an interactive and dynamic platform for all these diseases. This strategy allows visitors to be updated daily on all the latest news and interact with people internationally. This is essential, because due to the nature of these diseases, there is not a large concentration of individuals within any given proximity.
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